利用深度学习方法进行小儿癫痫病灶分割

A. Aminpour, Mehran Ebrahimi, E. Widjaja
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引用次数: 1

摘要

局灶性皮质发育不良(FCD)是导致耐药癫痫最常见的病变之一,经常被目视检查遗漏。FCD可以通过手术切除来实现癫痫的自由发作。通过改善病变检测,可以改善这些患者的手术效果。图像处理技术是改善癫痫手术前FCD检测的潜在工具。在这项研究中,我们提出并比较了两种类型的模型,完全卷积网络(FCN)和多序列FCN对耐药癫痫儿童的FCD进行分类和分割的性能。本实验采用体积t1加权、T2加权和FLAIR序列。整个切片FCN模型分别应用于每个序列,而多序列模型同时利用三个序列的组合信息。采用留一主体技术对模型进行训练和评价。我们评估了主观的敏感性和特异性,这对应于模型对那些有或没有病变的人进行分类的能力。我们还评估了病变的敏感性和特异性,表达了模型分割病变和骰子系数评估病变覆盖的能力。我们的数据包括80名FCD受试者(56名mr阳性,24名mr阴性)和15名健康对照。全层FCN在t1加权时表现最好,其次是t2加权,FLAIR序列表现最差。多序列模型优于T1全层FCN, MR阳性病例检出率分别为98%和93%,MR阴性病例检出率分别为92%和88%,MR阳性病例的病变覆盖率分别为74%和67%,MR阴性病例的病变覆盖率分别为68%和64%。多序列模型的骰子系数为57%,mr阳性病例的全切片FCN为56%。在6例新病例的测试队列中,多序列模型检测到6例中有4例预测病变与实际病变有56%的重叠。这项工作表明,深度学习方法,特别是全卷积网络,是一种很有前途的FCD分类和分割工具。需要进一步改进病变分类和分割,特别是对于小病变,以及在更大的多中心数据集上训练和测试最优算法。
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Lesion Segmentation in Paediatric Epilepsy Utilizing Deep Learning Approaches
Focal cortical dysplasia (FCD) is one of the most common lesions responsible for drug-resistant epilepsy, and is frequently missed by visual inspection. FCD may be amenable to surgical resection to achieve seizure freedom. By improving lesion detection the surgical outcome of these patients can be improved. Image processing techniques are a potential tool to improve the detection of FCD prior to epilepsy surgery. In this research, we propose and compare the performance of two type of models, Fully Convolutional Network (FCN) and a multi-sequence FCN to classify and segment FCD in children with drug-resistant epilepsy. This experiment utilized the volumetric T1-weighted, T2 weighted and FLAIR sequences. The whole slice FCN models were applied to each sequence separately while the multi-sequence model leverages combined information of all three sequences simultaneously. A leave-one-subject-out technique was utilized to train and evaluate the models. We evaluated subjectwise sensitivity and specificity, which corresponds to the ability of the model to classify those with or without a lesion. We also evaluated lesional sensitivity and specificity, which expresses the ability of the model to segment the lesion and the dice coefficient to evaluate lesion coverage. Our data consisted of 80 FCD subjects (56 MR-positive and 24 MR-negative) and 15 healthy controls. Performance of whole slice FCN was best on T1-weighted, followed by T2-weighted and lowest with FLAIR sequences. Multi-sequence model performed better than the T1 whole slice FCN, and detected 98% vs. 93% respectively MR-positive cases, and 92% vs. 88% respectively MR-negative cases, as well as achieved lesion coverage of 74% vs. 67% respectively for MR-positive cases and 68% vs. 64% for MR negative cases. The dice coefficient for the multi-sequence model was 57% and for whole slice FCN was 56% for MR-positive cases. In the test cohort of six new cases, the multi-sequence model detected 4 out of 6 cases where the predicted lesion had 56% overlap with the actual lesion. This work showed that deep learning methods in particular fully convolutional networks are a promising tool for classification and segmentation of FCD. Additional work is required to further improve lesion classification and segmentation, particularly for small lesions, as well as to train and test optimal algorithms on a larger multi-center dataset.
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